Canonical Allele Identifier: CA359707795
Gene: HCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645541T>G , CM000667.2:g.45645541T>G GRCh38
NC_000005.9:g.45645643T>G , CM000667.1:g.45645643T>G GRCh37
NC_000005.8:g.45681400T>G NCBI36
NG_042183.1:g.55578A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.493A>C MANE Select ENSP00000307342.4:p.Thr165Pro
ENST00000673735.1:c.493A>C ENSP00000501107.1:p.Thr165Pro
ENST00000303230.5:c.493A>C ENSP00000307342.4:p.Thr165Pro
ENST00000634658.1:c.493A>C ENSP00000489134.1:p.Thr165Pro
NM_021072.3:c.493A>C NP_066550.2:p.Thr165Pro
NM_021072.4:c.493A>C MANE Select NP_066550.2:p.Thr165Pro